-
Je něco špatně v tomto záznamu ?
Role of the TAP63 isoform in recurrent nasal polyps
A. Terrinoni, R. Palombo, C. Pitolli, S. Caporali, R. De Berardinis, S. Ciccarone, A. Lanzillotta, S. Mauramati, G. Porta, M. Minieri, G. Melino, S. Bernardini, E. Bruno
Jazyk angličtina Země Česko
Typ dokumentu časopisecké články
NLK
Free Medical Journals
od 2000
Freely Accessible Science Journals
od 2000
ProQuest Central
od 2005-01-01
Health & Medicine (ProQuest)
od 2005-01-01
ROAD: Directory of Open Access Scholarly Resources
od 2000
- MeSH
- fluorescenční protilátková technika MeSH
- lidé MeSH
- nádorové supresorové proteiny genetika metabolismus MeSH
- nosní polypy genetika metabolismus MeSH
- protein - isoformy genetika metabolismus MeSH
- regulace genové exprese u nádorů MeSH
- transkripční faktory Otx genetika metabolismus MeSH
- transkripční faktory genetika metabolismus MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
The pathogenic molecular mechanisms underlying the insurgence of nasal polyps has not been completely defined. In some patients, these lesions can have a recurrence after surgery removal, and the difference between recurrent and not recurrent patients is still unclear. To molecularly characterize and distinguish between these two classes, a cohort of patients affected by nasal polyposis was analysed. In all patients we analysed the p63 isoform expression using fresh tissues taken after surgery. Moreover, confocal immunofluorescence analysis of fixed sections was performed. The results show high ΔNp63 expression in samples from the nasal polyps of patients compared to the normal epithelia. Analysis of the expression level of the TAp63 isoform shows differential expression between the patients with recurrence compared to those not recurring. The data, considered as the ΔN/TAp63 ratio, really discriminate the two groups. In fact, even though ΔNp63 is expressed in non-recurrent patients, the resulting ratio ΔN/TAp63 is significantly lower in these patients. This clearly indicates that the status of TAp63 expression, represented by the ΔN/TAp63 ratio, could be considered a prognostic marker of low recurrence probability. In these samples we also investigated the expression of OTX2 transcription factor, known to be a selective activator of TAp63, detecting a significant correlation. Database analysis of HNSCC patients showed increased survival for the patients presenting OTX2 amplification and/or overexpression. These results, together with the fact that TAp63 can be selectively upregulated by HDAC inhibitors, open the possibility to consider local treatment of recurrent nasal polyps with these molecules.
Department of Clinical Sciences and Translational Medicine University of Rome Tor Vergata Rome Italy
Department of Experimental Medicine University of Rome Tor Vergata Rome Italy
Department of Industrial Engineering University of Rome Tor Vergata Rome Italy
Department of Medicine and Surgery University of Insubria Varese Italy
Literatura
- 000
- 00000naa a2200000 a 4500
- 001
- bmc20010294
- 003
- CZ-PrNML
- 005
- 20200721125336.0
- 007
- ta
- 008
- 200707s2019 xr ad f 000 0|eng||
- 009
- AR
- 035 __
- $a (PubMed)31903890
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xr
- 100 1_
- $a Terrinoni, A. $u Department of Experimental Medicine, University of Rome Tor Vergata, Rome, Italy
- 245 10
- $a Role of the TAP63 isoform in recurrent nasal polyps / $c A. Terrinoni, R. Palombo, C. Pitolli, S. Caporali, R. De Berardinis, S. Ciccarone, A. Lanzillotta, S. Mauramati, G. Porta, M. Minieri, G. Melino, S. Bernardini, E. Bruno
- 504 __
- $a Literatura
- 520 9_
- $a The pathogenic molecular mechanisms underlying the insurgence of nasal polyps has not been completely defined. In some patients, these lesions can have a recurrence after surgery removal, and the difference between recurrent and not recurrent patients is still unclear. To molecularly characterize and distinguish between these two classes, a cohort of patients affected by nasal polyposis was analysed. In all patients we analysed the p63 isoform expression using fresh tissues taken after surgery. Moreover, confocal immunofluorescence analysis of fixed sections was performed. The results show high ΔNp63 expression in samples from the nasal polyps of patients compared to the normal epithelia. Analysis of the expression level of the TAp63 isoform shows differential expression between the patients with recurrence compared to those not recurring. The data, considered as the ΔN/TAp63 ratio, really discriminate the two groups. In fact, even though ΔNp63 is expressed in non-recurrent patients, the resulting ratio ΔN/TAp63 is significantly lower in these patients. This clearly indicates that the status of TAp63 expression, represented by the ΔN/TAp63 ratio, could be considered a prognostic marker of low recurrence probability. In these samples we also investigated the expression of OTX2 transcription factor, known to be a selective activator of TAp63, detecting a significant correlation. Database analysis of HNSCC patients showed increased survival for the patients presenting OTX2 amplification and/or overexpression. These results, together with the fact that TAp63 can be selectively upregulated by HDAC inhibitors, open the possibility to consider local treatment of recurrent nasal polyps with these molecules.
- 650 _2
- $a fluorescenční protilátková technika $7 D005455
- 650 _2
- $a regulace genové exprese u nádorů $7 D015972
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a nosní polypy $x genetika $x metabolismus $7 D009298
- 650 _2
- $a transkripční faktory Otx $x genetika $x metabolismus $7 D051857
- 650 _2
- $a protein - isoformy $x genetika $x metabolismus $7 D020033
- 650 _2
- $a transkripční faktory $x genetika $x metabolismus $7 D014157
- 650 _2
- $a nádorové supresorové proteiny $x genetika $x metabolismus $7 D025521
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Palombo, R. $u Department of Experimental Medicine, University of Rome Tor Vergata, Rome, Italy
- 700 1_
- $a Pitolli, C. $u Department of Clinical Sciences and Translational Medicine, University of Rome Tor Vergata, Rome, Italy
- 700 1_
- $a Caporali, S. $u Department of Industrial Engineering, University of Rome Tor Vergata, Rome, Italy
- 700 1_
- $a De Berardinis, R. $u Department of Clinical Sciences and Translational Medicine, University of Rome Tor Vergata, Rome, Italy
- 700 1_
- $a Ciccarone, S. $u Department of Clinical Sciences and Translational Medicine, University of Rome Tor Vergata, Rome, Italy
- 700 1_
- $a Lanzillotta, A. $u Department of Clinical Sciences and Translational Medicine, University of Rome Tor Vergata, Rome, Italy
- 700 1_
- $a Mauramati, S. $u University of Pavia, Italy and Department of Otorhinolaryngology, University of Pavia, Foundation IRCCS Policlinico "San Matteo", Pavia, Italy
- 700 1_
- $a Porta, G. $u Department of Medicine and Surgery, University of Insubria, Varese, Italy
- 700 1_
- $a Minieri, M. $u Department of Experimental Medicine, University of Rome Tor Vergata, Rome, Italy
- 700 1_
- $a Melino, G. $u Department of Experimental Medicine, University of Rome Tor Vergata, Rome, Italy
- 700 1_
- $a Bernardini, S. $u Department of Industrial Engineering, University of Rome Tor Vergata, Rome, Italy
- 700 1_
- $a Bruno, E. $u Department of Clinical Sciences and Translational Medicine, University of Rome Tor Vergata, Rome, Italy
- 773 0_
- $w MED00011004 $t Folia biologica $x 0015-5500 $g Roč. 65, č. 4 (2019), s. 170-180
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/31903890 $y Pubmed
- 856 41
- $u https://fb.cuni.cz/file/5902/fb2019a0017.pdf $y plný text volně přístupný
- 910 __
- $a ABA008 $b A 970 $c 89 $y p $z 0
- 990 __
- $a 20200707 $b ABA008
- 991 __
- $a 20200710132211 $b ABA008
- 999 __
- $a ok $b bmc $g 1546289 $s 1100386
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2019 $b 65 $c 4 $d 170-180 $i 0015-5500 $m Folia biologica (Praha) $n Folia biol. (Praha) $x MED00011004
- LZP __
- $b NLK118 $a Pubmed-20200707